| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.78625057A>G | CA7684689 | CHRNB4 | c.*76T>C (n.*76T>C) c.594T>C (p.Ala198=) c.777T>C (p.Ala259=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.78625057A>T | CA715980697 | CHRNB4 | c.*76T>A (n.*76T>A) c.594T>A (p.Ala198=) c.777T>A (p.Ala259=) | dbSNP gnomAD v4 |
| 15 | g.78625057A= | CA2189571000 | CHRNB4 | c.*76T= (n.*76T=) c.594T= (p.Ala198=) c.777T= (p.Ala259=) | dbSNP |